A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6458882



Internal ID21116435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:50709901..50821300hg38UCSC Ensembl
chr11:50669072..50780471hg19UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38111400
hg19111400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1143n223
Supporting Variantsnssv18192801
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6458882
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer